Researcher
Jeroen Van Houdt
- Disciplines:Genetics, Systems biology, Molecular and cell biology
Affiliations
- Biomedical Sciences Research Coördination (Section)
Member
From1 Feb 2012 → 31 Dec 2012 - Laboratory for Cytogenetics and Genome Research (Division)
Member
From1 Nov 2009 → 31 Jan 2014 - Ecology, Evolution and Biodiversity Conservation (Division)
Member
From1 Oct 1999 → 31 May 2007
Projects
1 - 1 of 1
- Behavioral and genomic aspects of cichlid speciation (GENBAS).From1 Dec 2013 → 31 Oct 2019Funding: BRAIN-be(Belgian Research Action through Interdisciplinary Networks)
Publications
11 - 20 of 48
- Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities(2015)
Authors: Mala Isrie, Masoud Zamani Esteki, Hilde Peeters, Thierry Voet, Jeroen Van Houdt, Wim Van Paesschen, Hilde Van Esch
Pages: 205 - 10 - Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities(2015)
Authors: Mala Isrie, Masoud Zamani Esteki, Hilde Peeters, Thierry Voet, Jeroen Van Houdt, Wim Van Paesschen, Hilde Van Esch
Pages: 205 - 10 - Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management(2015)
Authors: Baran Bayindir, Luc Dehaspe, Nathalie Brison, Paul Brady, Simon Ardui, Molka Kammoun, Lars Van der Veken, Klaske Lichtenbelt, Kris Van den Bogaert, Jeroen Van Houdt, et al.
Pages: 1286 - 1293 - GBSX: a toolkit for experimental design and demultiplexing genotyping by sequencing experiments(2015)
Authors: Matthew Hestand, Joris Vermeesch, Jeroen Van Houdt
Pages: 73 - Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management(2015)
Authors: Baran Bayindir, Nathalie Brison, Paul Brady, Simon Ardui, Molka Kammoun, Kris Van Den Bogaert, Jeroen Van Houdt, Hilde Peeters, Hilde Van Esch, Thomy de Ravel de l'Argentière, et al.
Pages: 1286 - 1293 - GBSX: a toolkit for experimental design and demultiplexing genotyping by sequencing experiments(2015)
Authors: Koen Herten, Matthew Hestand, Joris Vermeesch, Jeroen Van Houdt
Pages: 73 - Pseudoautosomal Region 1 length polymorphism in the human population(2014)
Authors: Matthew Hestand, Maarten Larmuseau, Mala Isrie, Erika Souche, Jeroen Van Houdt, Hilde Van Esch, Koenraad Devriendt, Thierry Voet, Ronny Decorte, Joris Vermeesch
- NGS-Logistics: Federated analysis of NGS sequence variants across multiple locations(2014)
Authors: Amin Ardeshirdavani, Erika Souche, Jeroen Van Houdt, Joris Vermeesch, Yves Moreau
Pages: 71 - 73 - Microsatellite primers for the gynodioecious grassland perennial Saxifraga granulata (Saxifragaceae)(2014)
Authors: Sascha van der Meer, Jeroen Van Houdt, Gregory Maes, Hans Jacquemyn
- Exome sequencing identifies ZFPM2 as a cause of familial isolated Congenital Diaphragmatic Hernia and possibly cardiovascular malformations(2014)
Authors: Paul Brady, Jeroen Van Houdt, Jan Deprest, Koenraad Devriendt, Joris Vermeesch
Pages: 247 - 252
Patents
1 - 2 of 2